Package 68682-392-02
Brand: hydrocortisone butyrate
Generic: hydrocortisone butyratePackage Facts
Identity
Package NDC
68682-392-02
Digits Only
6868239202
Product NDC
68682-392
Description
1 BOTTLE in 1 CARTON (68682-392-02) / 59 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
hydrocortisone butyrate
Generic
hydrocortisone butyrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2f38330f-dede-a2af-e063-6294a90a1a94", "openfda": {"unii": ["05RMF7YPWN"], "rxcui": ["1370763"], "spl_set_id": ["dde66620-657b-4b30-bd30-4bb6e83612cb"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68682-392-02) / 59 mL in 1 BOTTLE", "package_ndc": "68682-392-02", "marketing_start_date": "20180608"}], "brand_name": "HYDROCORTISONE BUTYRATE", "product_id": "68682-392_2f38330f-dede-a2af-e063-6294a90a1a94", "dosage_form": "LOTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68682-392", "generic_name": "HYDROCORTISONE BUTYRATE", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCORTISONE BUTYRATE", "active_ingredients": [{"name": "HYDROCORTISONE BUTYRATE", "strength": "1 mg/mL"}], "application_number": "NDA022076", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180608", "listing_expiration_date": "20261231"}